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1,1,1,2,2,3,3,4,4,5,5-undecamethylpentasilane | 79107-95-2

中文名称
——
中文别名
——
英文名称
1,1,1,2,2,3,3,4,4,5,5-undecamethylpentasilane
英文别名
——
1,1,1,2,2,3,3,4,4,5,5-undecamethylpentasilane化学式
CAS
79107-95-2
化学式
C11H34Si5
mdl
——
分子量
306.818
InChiKey
KIDQSHZRGHQCLY-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    251.2±23.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.25
  • 重原子数:
    16.0
  • 可旋转键数:
    4.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis, structure, and reactivity of hydridobis(silylene)ruthenium(IV)-xantsil complexes (xantsil = (9,9-dimethylxanthene-4,5-diyl)bis(dimethylsilyl)) — A stabilized form of key intermediates in the catalytic oligomerization–deoligomerization of hydrosilanes
    作者:Masaaki Okazaki、Jim Josephus Gabrillo Minglana、Nobukazu Yamahira、Hiromi Tobita、Hiroshi Ogino
    DOI:10.1139/v03-151
    日期:2003.11.1

    Ruκ2(Si,Si)-xantsil}(CO)(η6-C6H5CH3) (1) was found to be a catalyst for oligomerization–deoligomerization of HSiMe2SiMe3 to give H(SiMe2)nMe (n = 1–8 at 90 °C for 2 days). Treatment of 1 with HSiMe2SiMe2OR (R = Me, t-Bu) led to quantitative formation of Ruκ3(O,Si,Si)-xantsil}(CO)(H)(SiMe2•••O(R)•••SiMe2)} (R = Me (2a), t-Bu (2b)), which also worked as a catalyst for oligomerization–deoligomerization of HSiMe2SiMe3. Based on these experimental results, a mechanism involving silyl(silylene) intermediates was proposed for the oligomerization–deoligomerization of HSiMe2SiMe3. Complex 2a reacted with MeOH in toluene-d8 to give Ruκ2(Si,Si)-xantsil}(CO)(η6-toluene-d8) and Me2Si(OMe)2 with evolution of H2. Under a CO atmosphere, 2a was smoothly converted to its CO adduct Ruκ2(Si,Si)-xantsil}(CO)2(H)(SiMe2•••O(Me)•••SiMe2)} (3).Key words: silylene complex, ruthenium, polysilane, dehydrogenative coupling, oligomerization.

    已发现 Ruκ2(Si,Si)-xantsil}(CO)(η6-C6H5CH3) (1) 是 HSiMe2SiMe3 的寡聚-去聚合催化剂,在90°C处理2天后生成 H(SiMe2)nMe (n = 1–8)。将1与HSiMe2SiMe2OR (R = Me, t-Bu) 反应,可定量生成 Ruκ3(O,Si,Si)-xantsil}(CO)(H)(SiMe2•••O(R)•••SiMe2)} (R = Me (2a), t-Bu (2b)),也可作为 HSiMe2SiMe3 的寡聚-去聚合催化剂。基于这些实验结果,提出了涉及硅烷(烯)中间体的寡聚-去聚合机理。在甲苯-d8中,2a 与 MeOH 反应生成 Ruκ2(Si,Si)-xantsil}(CO)(η6-甲苯-d8) 和 Me2Si(OMe)2,伴随释放 H2。在 CO 气氛下,2a 顺利转化为其 CO 加合物 Ruκ2(Si,Si)-xantsil}(CO)2(H)(SiMe2•••O(Me)•••SiMe2)} (3)。关键词:烯配合物、、聚硅烷、脱氢偶联、寡聚合。

  • Coordinatively Unsaturated Ru(II) Species Ru(xantsil)(CO): A New Active Catalyst for Oligomerization/Deoligomerization of HSiMe<sub>2</sub>SiMe<sub>3</sub>[xantsil=(9,9-Dimethylxanthene-4,5-diyl)bis(dimethylsilyl)]. Isolation of a Stabilized Form of the Silyl(silylene) Intermediates
    作者:Jim Josephus G. Minglana、Masaaki Okazaki、Hiromi Tobita、Hiroshi Ogino
    DOI:10.1246/cl.2002.406
    日期:2002.3
    Ru(xantsil)(CO)(η6-C6H5CH3) (1) was found to be a catalyst for the oligomerization/deoligomerization of HSiMe2SiMe3 to give H(SiMe2)nMe (n=1–8). A possible mechanism involving a silyl(silylene) intermediate was strongly supported by the isolation of its stabilized form, i.e., alkoxy-bridged bis(silylene) complex which was characterized by X-ray crystal structure analysis.
    Ru(xantsil)(CO)(η6-C6H5CH3) (1) 被发现是一种催化剂,用于 HSiMe2SiMe3 的低聚合/解聚反应,生成 H(SiMe2)nMe (n=1–8)。一种涉及烯(silylene)中间体的可能机制得到了强有力的支持,因为其稳定形式,即通过醇氧桥连的双(烯)络合物被分离出来,并通过X射线晶体结构分析进行了表征。
  • Nefedov, O. M.; Skell, Philip S., Doklady Chemistry, 1981, vol. 259, p. 320 - 322
    作者:Nefedov, O. M.、Skell, Philip S.
    DOI:——
    日期:——
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